Product Recalls in Iowa
Product recalls affecting Iowa — including food, drugs, consumer products, medical devices, and vehicles distributed to Iowa. RecallDetector monitors distribution data from the FDA, USDA, CPSC, and NHTSA to show you which recalls are relevant to your area. 2,475 recalls have been distributed to Iowa in the last 12 months.
Showing 22341–22360 of 49,990 recalls
Recalled Item: Dominator Flour 50lb bags Product Code 745220 Lot#: 8319BF Recalled by ADM -...
The Issue: potential presence of E. coli. O26
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: Gigantic Flour 50lbs Product Code 701220 Lot #: 8346BF Recalled by ADM -...
The Issue: potential presence of E. coli. O26
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: Springup Flr Enr Recalled by ADM - CHICAGO Due to Potential E. coli...
The Issue: potential presence of E. coli. O26
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: Gold Medal Flour Mt Bulk Product Code 805046 Recalled by ADM - CHICAGO Due...
The Issue: potential presence of E. coli. O26
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: Hancock II T510 Bioprosthesis Recalled by Medtronic Inc Due to Mislabeling
The Issue: Fifteen affected devices were distributed worldwide, which were mislabeled...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Mosaic 310 Bioprosthesis Recalled by Medtronic Inc Due to Mislabeling
The Issue: Fifteen affected devices were distributed worldwide, which were mislabeled...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: LVivo EF app on Vscan Extend. Sold under the following Recalled by GE...
The Issue: Overestimation bias in automatically calculated ejection fraction (EF)...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Hancock II T510 Bioprosthesis Recalled by Medtronic Inc Due to Mislabeling
The Issue: Fifteen affected devices were distributed worldwide, which were mislabeled...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Mosaic 310 Bioprosthesis Recalled by Medtronic Inc Due to Mislabeling
The Issue: Fifteen affected devices were distributed worldwide, which were mislabeled...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Hancock II T510 Bioprosthesis Recalled by Medtronic Inc Due to Mislabeling
The Issue: Fifteen affected devices were distributed worldwide, which were mislabeled...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: DRG Salivary Testosterone ELISA- IVD for the detection of Testerone Recalled...
The Issue: Salivary assay may observe a higher percentage of samples with 0 pg/ml...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: The Alinity ci-series System Control Modules which are configured with...
The Issue: All versions of the Alinity ci-series software may not detect an issue on...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: AMIKACIN SULFATE INJECTION Recalled by Heritage Pharmaceuticals, Inc. Due to...
The Issue: Non-Sterility:Microbial growth detected in sub lot of Amikacin Sulfate...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: PROCHLORPERAZINE EDISYLATE INJECTION Recalled by Heritage Pharmaceuticals,...
The Issue: Non-Sterility:Microbial growth detected in sub lot of Amikacin Sulfate...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: The device is a 25-gauge infusion line that is part Recalled by Dutch...
The Issue: Labeled 25-gauge surgical pack, TDC Vitrectomy Pack VGPC 25g, containing...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Guardian Connect App CSS7200 iOS and Guardian Connect Transmitter GST4C...
The Issue: Customers using the firm's continuous glucose monitoring system application...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Getinge 86-Series-Medical Washer-Disinfector Part Number: S-86662003 Product...
The Issue: Possibility that inlet pump hose of the Washer Disinfector Getinge 86-Series...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: The Visibly Online Vision Test which is part of Recalled by Opternative Inc...
The Issue: Lack of 510K clearance
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Getinge 86-Series-Medical Washer-Disinfector Part Number: S-86682003 Product...
The Issue: Possibility that inlet pump hose of the Washer Disinfector Getinge 86-Series...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Suja Organic Kombucha - Variety Pack: 6 x 15.2 oz. glass bottle Recalled by...
The Issue: Firm has received complaints of finding pieces of glass in the products.
Recommended Action: Do not consume. Return to store for a refund or discard.